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Practicality of Identifying Mitochondria Variants From Exome and RNAseq Data

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Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease

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Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease

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A Probabilistic Method for Identifying Rare Variants Underlying Complex Traits

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An Improved Burden-Test Pipeline for Identifying Associations From Rare Germline and Somatic Variants

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Whole Exome Sequencing of Rare Variants in EIF4G1 and VPS35 in Parkinson Disease

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Exome Chip Meta-Analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

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Using Whole-Exome Sequencing to Identify Variants Inherited From Mosaic Parents

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Whole Exome Analyses to Examine the Impact of Rare Variants on Left Ventricular Traits in African American Participants From the HyperGEN and GENOA Studies

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